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Summary Literature (0)
MIM:617854 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 56; MRD56


Xenbase Genes: cltc

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030922 - intellectual disability, autosomal dominant 56

Disease Ontology (DO):
DOID:0080226 - autosomal dominant intellectual developmental disorder 56